Amlodipine Besylate
- Product NDC
- 64980-392
- 11-digit product format
- 649800392
- Labeler code
- 64980
- Product ID
- 64980-392_81ee1d2e-7520-4de1-b8ee-60186c11c3e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- Application
- ANDA078021
- Marketing category
- ANDA
- Marketing start
- 2017-11-07
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record